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MMEP syndrome

Just diagnosed with MMEP syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees MMEP syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full MMEP syndrome hub →

Overview

MMEP syndrome is a rare condition. Also known as MCOPS8, Microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome, Syndromic microphthalmia type 8, Viljoen-Smart syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for MMEP syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:3434 · OMIM 601349 · ICD-10 Q87.8 · GARD 0003693

Find care for MMEP syndrome

Authoritative references for MMEP syndrome

Common questions

I was just diagnosed with MMEP syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees MMEP syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for MMEP syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat MMEP syndrome, filtered to your area.

Are there clinical trials for MMEP syndrome?

Tomeko shows live, recruiting studies for MMEP syndrome from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com